510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900518Substantially Equivalent

Blom-Singer(r) Tracheoesophageal Puncture Kit

Freudenberg Medical, LLC, Santa Barbera CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900518 is the FDA 510(k) clearance record for BLOM-SINGER(R) TRACHEOESOPHAGEAL PUNCTURE KIT, a class II device, cleared for Helix Medical, Inc. on under FDA product code EWL (Prosthesis, Laryngeal (Taub)). FDA records list 21 510(k) clearances for Freudenberg Medical, LLC, from to . As of , FDA records show no recalls naming K900518.

Clearance record

Decision date
Received
(132 days to decision)
Product code
EWL Prosthesis, Laryngeal (Taub)
Regulation
21 CFR 874.3730
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Helix Medical, Inc. 210 Santa Barbera St., Santa Barbera CA
Third party review
No

Clearances, product code EWL

Trailing 12 months

FDA records hold no clearances under product code EWL in the trailing twelve months.

FDA records show no clearances under product code EWL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EWL, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260